Sr Central Monitoring Analyst II at Thermo Fisher Scientific

Essential Functions:  

• Ensures performance of assigned reviews with high quality, on-time results with more complex analyses or deeper root cause analyses to connect related signal to risks.
• Provides training and guidance to junior team members.
• May participate in a project lead or development specialist role, or a combination of both.
• Project leadership activities include: Leads the design and setup of study specific tools and centralized monitoring plan for data review; manages review timelines, develops analysis assignments for team, and supports budget management; organizes, communicates with internal team, and delegates as appropriate to ensure reviews are completed on-time, on budget, with high quality; assists with report development, delivers reports, and leads centralized monitoring meetings; contributes to risk assessment through the completion of the department risk assessment tools. Participates in the cross-functional risk assessment review meetings and contributes to overall risk planning.
• Specialist activities included focused efforts on the development of new tools and analyses within area of specialty.

Education and Experience: 

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years’).
• Prior experience in clinical monitoring, data management, biostatistics or related field in support of clinical trials is preferred.